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临床试验/ACTRN12613001103752
ACTRN12613001103752已完成未知

Randomised controlled trial of tissue adhesive, absorbent dressings or external stabilisation devices versus standard care (bordered polyurethane) dressings to prevent central venous access device failure in hospital patients with central venous access devices: the CASCADE trial

Griffith University0 个研究点目标入组 2,444 人开始时间: 2013年10月2日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
2,444

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Open (masking not used)

入排标准

年龄范围
o limit 至 o limit(—)
性别
All

入选标准

  • 1. Informed written consent
  • 2. CVAD to be inserted for clinical care (includes peripherally inserted central catheters, percutaneous central catheters, tunnelled central catheters).

排除标准

  • 1. Current bloodstream infection
  • 2. Non-English speaking patients without interpreter
  • 3. CVADS inserted through diseased, burned or scarred skin
  • 4. Current skin tear/'paper' skin at high risk of tear
  • 5. Known allergy to any study product
  • 6. Extremely diaphoretic patients

研究者

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